Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 67119408 | HCID 67119408 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Flometoquin | HCID 67119441 | 91.4% |
Reaction Steps
Dimethyl acetamide (980 ml) and 98 g of 2-ethyl-3,7-dimethyl-6-(4-(trifluoromethoxy)phenoxy)quinolin-4(1H)-one were charged into a glass flask equipped with a stirring device, a thermometer, a reflux condenser, and a calcium chloride tube and having a volume of 2000 ml under a nitrogen atmosphere, and the mixture was cooled to 15° C. 55% sodium hydride (18.2 g) was added thereto, and the mixture was stirred at 15 to 20° C. for one hr. Methyl chloroformate (32.1 g) was added dropwise, and a reaction was allowed to proceed at room temperature for one hr. The reaction mixture was poured into 5 L of ice water contained in a 10-L plastic container, and the mixture was stirred at room temperature for 2 hr. The precipitated solid was collected by a suction filter and was washed with n-hexane and water. The solid was dried in vacuo to give 2-ethyl-3,7-dimethyl-6-(4-(trifluoromethoxy)phenoxy)quinolin-4-yl methyl carbonate (103.3 g, yield 91.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126934B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-c93b792a0d774eb6869aba272a789b5a |
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| Source note | uspto-grants-2015_09 |
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